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Mutation:
VRK2 S415N
Summary
Clinical Information
Cancer types: (TCGA MC3)
UCEC
Cancer types: (PCAWG)
Uterus-AdenoCA
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 419K
Affected site:
Position: 419
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
420T | EVNSFPQK[I/T]ISYTQFP | 1 |
proximal
|
415N | EVN[S/N]SFPQKISYTQFP | 4 |
distal
|
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